Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| A0A2R8Y535 | ATP2B2 | ATPase plasma membrane Ca2+ transporting … | Homo sapiens (Human) | 387 aa |
Protein Details: A0A2R8Y535 (ATP2B2)
Protein Information
| Accession | A0A2R8Y535 |
|---|---|
| Protein Names | ATPase plasma membrane Ca2+ transporting 2 |
| Gene Symbol | ATP2B2 |
| Organism | Homo sapiens (Human) |
| Length | 387 aa |
| Isoforms | No isoforms |
| Related PMIDs | 26876311 |
| Database Sources | No database sources |
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
Experimental Database High Prediction Non-palmitylated Cys
1-501GPALKKADVG11FAMGIAGTDV21AKEASDIILT31DDNFSSIVKA41VMWGRNVYDS
51-10051ISKFLQFQLT61VNVVAVIVAF71TGACITQDSP81LKAVQMLWVN91LIMDTFASLA
101-150101LATEPPTETL111LLRKPYGRNK121PLISRTMMKN131ILGHAVYQLA141LIFTLLFVGE
151-200151KMFQIDSGRN161APLHSPPSEH171YTIIFNTFVM181MQLFNEINAR191KIHGERNVFD
201-250201GIFRNPIFCT211IVLGTFAIQI221VIVQFGGKPF231SCSPLQLDQW241MWCIFIGLGE
251-300251LVWGQSRIGC261LQGPVTSGGI271RDRGISNPRR281TEGQPRARLM291QDELDPPPCP
301-350301VLTMPRAAPT311LQLGKPKLGH321RHHPDQQTQV331PQGGRQAHTE341GGDPGGGAQR
351-387351GRGGDRPRGA361GAAAGPDPVV371PRPESDPDTD381PRREGVP
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 74 | - | - | - |
GPS-Palm: 0.86
Deep-Palm: 0.92
|
|
| 209 | - | - | - |
Deep-Palm: 0.38
|
|
| 232 | - | - | - |
GPS-Palm: 0.88
Deep-Palm: 0.08
|
|
| 243 | - | - | - |
Deep-Palm: 0.10
|
|
| 260 | - | - | - |
GPS-Palm: 0.76
Deep-Palm: 0.94
|
|
| 299 | - | - | - |
Deep-Palm: 0.82
|
Score Interpretation:
• GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
• Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
• GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
• Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
1
frontal cortex
Specificity: 1.000
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID).
Blue bars: Literature data, Orange bars: Mass Spectrometry data.
The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
TCGA Cysteine Mutation Information
Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.
| Position | Amino Acid Change | Frequency | Type | Function | Cancer Type |
|---|---|---|---|---|---|
| 32 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 32 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 59 | R → C | 0.002294 | SNP | Missense Mutation | OV |
| 86 | F → C | 0.007299 | SNP | Missense Mutation | READ |
| 151 | W → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 185 | R → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 249 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 249 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 432 | C → S | 0.006944 | SNP | Missense Mutation | TGCT |
| 491 | G → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 497 | C → S | 0.001764 | SNP | Missense Mutation | LUAD |
| 559 | G → C | 0.002288 | SNP | Missense Mutation | STAD |
| 588 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 597 | Y → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 606 | R → C | 0.001969 | SNP | Missense Mutation | HNSC |
| 606 | R → C | 0.002020 | SNP | Missense Mutation | PRAD |
| 606 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 621 | R → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 621 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 651 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 666 | C → C | 0.001887 | SNP | Silent | UCEC |
| 673 | C → C | 0.001887 | SNP | Silent | UCEC |
| 677 | R → C | 0.005435 | SNP | Missense Mutation | ESCA |
| 699 | C → C | 0.001887 | SNP | Silent | UCEC |
| 869 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1014 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1020 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1055 | S → C | 0.002747 | SNP | Missense Mutation | LIHC |
| 1067 | C → C | 0.003460 | SNP | Silent | CESC |
| 1142 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 1178 | S → C | 0.002294 | SNP | Missense Mutation | OV |
| 1211 | S → C | 0.001764 | SNP | Missense Mutation | LUAD |